Incidental Mutation 'IGL02666:Tcaf2'
ID 302759
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Tcaf2
Ensembl Gene ENSMUSG00000029851
Gene Name TRPM8 channel-associated factor 2
Synonyms Fam115c
Accession Numbers
Essential gene? Probably non essential (E-score: 0.105) question?
Stock # IGL02666
Quality Score
Status
Chromosome 6
Chromosomal Location 42599950-42622134 bp(-) (GRCm39)
Type of Mutation splice site
DNA Base Change (assembly) C to A at 42606058 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000031879 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000031879]
AlphaFold Q921K8
Predicted Effect probably benign
Transcript: ENSMUST00000031879
SMART Domains Protein: ENSMUSP00000031879
Gene: ENSMUSG00000029851

DomainStartEndE-ValueType
low complexity region 515 526 N/A INTRINSIC
M60-like 543 842 4.85e-138 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000131341
Coding Region Coverage
Validation Efficiency
Allele List at MGI

All alleles(1) : Targeted(1)

Other mutations in this stock
Total: 49 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
9230109A22Rik T C 15: 25,138,944 (GRCm39) noncoding transcript Het
Abca15 G A 7: 119,934,431 (GRCm39) V136M probably damaging Het
Abhd3 A G 18: 10,645,148 (GRCm39) I382T probably benign Het
Cux1 C A 5: 136,304,169 (GRCm39) E1336* probably null Het
Cyb5r3 T C 15: 83,044,554 (GRCm39) I155V probably damaging Het
Ddx24 T C 12: 103,390,314 (GRCm39) T226A possibly damaging Het
Dld T C 12: 31,382,408 (GRCm39) N465S probably null Het
Dnmbp A G 19: 43,842,566 (GRCm39) probably benign Het
Dock9 T C 14: 121,818,111 (GRCm39) H1580R probably benign Het
Drd3 C A 16: 43,637,319 (GRCm39) probably benign Het
Gabrb2 G T 11: 42,420,322 (GRCm39) probably null Het
Gbp9 T C 5: 105,242,141 (GRCm39) probably null Het
Inhba A T 13: 16,201,664 (GRCm39) I409F possibly damaging Het
Iqgap2 T C 13: 95,764,564 (GRCm39) N1560S probably damaging Het
Itsn1 A G 16: 91,617,606 (GRCm39) probably benign Het
Kat6b T C 14: 21,678,938 (GRCm39) F434L probably damaging Het
Klra1 A G 6: 130,341,278 (GRCm39) C232R probably damaging Het
Krt18 T A 15: 101,938,302 (GRCm39) I175N probably damaging Het
Lck A G 4: 129,450,212 (GRCm39) V178A probably damaging Het
Mroh4 C A 15: 74,481,624 (GRCm39) G737V probably benign Het
Mug2 A C 6: 122,058,285 (GRCm39) L1282F probably damaging Het
Myo9a A G 9: 59,832,187 (GRCm39) N2572S probably benign Het
Nup88 G T 11: 70,834,695 (GRCm39) probably benign Het
Nxph3 G T 11: 95,401,834 (GRCm39) H193Q possibly damaging Het
Or5b97 G T 19: 12,878,221 (GRCm39) H308N probably benign Het
Orm2 A G 4: 63,283,970 (GRCm39) T198A possibly damaging Het
Pom121 T C 5: 135,415,686 (GRCm39) I397V unknown Het
Prex1 C A 2: 166,414,909 (GRCm39) E1313D probably benign Het
Prkg2 T A 5: 99,145,378 (GRCm39) probably benign Het
Prl2a1 A T 13: 27,990,310 (GRCm39) K86N possibly damaging Het
Ptpro G A 6: 137,355,057 (GRCm39) S188N probably damaging Het
Ptprz1 A T 6: 23,001,209 (GRCm39) I1100F probably benign Het
Ryr1 C A 7: 28,719,188 (GRCm39) M4406I unknown Het
Sdf4 T A 4: 156,093,281 (GRCm39) Y204* probably null Het
Serinc1 A T 10: 57,400,089 (GRCm39) probably null Het
Slc39a5 C T 10: 128,234,324 (GRCm39) R193H probably damaging Het
Smad9 A G 3: 54,689,888 (GRCm39) K36R probably damaging Het
Spam1 T A 6: 24,796,123 (GRCm39) L25I possibly damaging Het
Stab2 A T 10: 86,686,766 (GRCm39) S809R possibly damaging Het
Szt2 G A 4: 118,231,252 (GRCm39) R35C probably damaging Het
Tfap2d A C 1: 19,174,979 (GRCm39) D144A probably benign Het
Tmprss11d A T 5: 86,479,052 (GRCm39) V117D probably damaging Het
Tnxb A G 17: 34,903,913 (GRCm39) D1141G probably benign Het
Traf6 A T 2: 101,527,512 (GRCm39) T421S possibly damaging Het
Txndc16 G A 14: 45,448,607 (GRCm39) probably benign Het
Utp25 G A 1: 192,789,904 (GRCm39) Q752* probably null Het
Vmn1r73 C A 7: 11,490,865 (GRCm39) P228T probably damaging Het
Vmn2r4 A G 3: 64,296,433 (GRCm39) I784T probably benign Het
Zfp420 A G 7: 29,573,795 (GRCm39) D5G probably benign Het
Other mutations in Tcaf2
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00333:Tcaf2 APN 6 42,606,970 (GRCm39) nonsense probably null
IGL00909:Tcaf2 APN 6 42,601,510 (GRCm39) missense probably damaging 1.00
IGL01448:Tcaf2 APN 6 42,607,262 (GRCm39) missense probably benign 0.05
IGL01870:Tcaf2 APN 6 42,601,411 (GRCm39) missense possibly damaging 0.47
IGL02133:Tcaf2 APN 6 42,604,330 (GRCm39) missense probably benign 0.06
IGL02208:Tcaf2 APN 6 42,606,020 (GRCm39) missense probably damaging 1.00
jiaozhi UTSW 6 42,603,371 (GRCm39) missense probably damaging 1.00
PIT4260001:Tcaf2 UTSW 6 42,619,739 (GRCm39) missense probably damaging 0.97
PIT4382001:Tcaf2 UTSW 6 42,601,300 (GRCm39) makesense probably null
R0029:Tcaf2 UTSW 6 42,607,093 (GRCm39) nonsense probably null
R0029:Tcaf2 UTSW 6 42,607,093 (GRCm39) nonsense probably null
R0047:Tcaf2 UTSW 6 42,606,547 (GRCm39) missense probably benign
R0047:Tcaf2 UTSW 6 42,606,547 (GRCm39) missense probably benign
R0255:Tcaf2 UTSW 6 42,619,838 (GRCm39) missense possibly damaging 0.95
R0617:Tcaf2 UTSW 6 42,619,445 (GRCm39) missense probably damaging 0.97
R1387:Tcaf2 UTSW 6 42,601,512 (GRCm39) missense probably damaging 1.00
R1523:Tcaf2 UTSW 6 42,601,385 (GRCm39) nonsense probably null
R1529:Tcaf2 UTSW 6 42,606,440 (GRCm39) missense probably benign 0.03
R1698:Tcaf2 UTSW 6 42,604,951 (GRCm39) nonsense probably null
R1992:Tcaf2 UTSW 6 42,606,791 (GRCm39) missense probably benign
R2065:Tcaf2 UTSW 6 42,604,981 (GRCm39) missense probably benign 0.12
R2144:Tcaf2 UTSW 6 42,619,738 (GRCm39) missense probably benign 0.45
R2435:Tcaf2 UTSW 6 42,607,298 (GRCm39) missense possibly damaging 0.72
R2519:Tcaf2 UTSW 6 42,606,365 (GRCm39) missense possibly damaging 0.92
R3979:Tcaf2 UTSW 6 42,619,481 (GRCm39) missense probably damaging 1.00
R4093:Tcaf2 UTSW 6 42,619,772 (GRCm39) missense probably damaging 1.00
R4532:Tcaf2 UTSW 6 42,603,371 (GRCm39) missense probably damaging 1.00
R4780:Tcaf2 UTSW 6 42,604,996 (GRCm39) missense probably damaging 1.00
R4906:Tcaf2 UTSW 6 42,606,679 (GRCm39) missense probably benign 0.02
R4993:Tcaf2 UTSW 6 42,619,574 (GRCm39) missense probably damaging 1.00
R5076:Tcaf2 UTSW 6 42,606,401 (GRCm39) missense probably benign 0.16
R5643:Tcaf2 UTSW 6 42,619,707 (GRCm39) missense possibly damaging 0.85
R5644:Tcaf2 UTSW 6 42,619,707 (GRCm39) missense possibly damaging 0.85
R5975:Tcaf2 UTSW 6 42,619,712 (GRCm39) missense probably benign 0.22
R6234:Tcaf2 UTSW 6 42,607,308 (GRCm39) missense probably benign
R6269:Tcaf2 UTSW 6 42,604,342 (GRCm39) missense probably damaging 1.00
R6276:Tcaf2 UTSW 6 42,606,687 (GRCm39) missense probably benign 0.04
R6375:Tcaf2 UTSW 6 42,603,112 (GRCm39) missense probably damaging 0.99
R6523:Tcaf2 UTSW 6 42,619,953 (GRCm39) missense probably benign 0.01
R6825:Tcaf2 UTSW 6 42,606,452 (GRCm39) missense probably benign 0.05
R7039:Tcaf2 UTSW 6 42,603,074 (GRCm39) missense probably damaging 1.00
R7099:Tcaf2 UTSW 6 42,607,275 (GRCm39) missense probably benign 0.02
R7284:Tcaf2 UTSW 6 42,606,472 (GRCm39) missense probably damaging 1.00
R7822:Tcaf2 UTSW 6 42,606,033 (GRCm39) missense possibly damaging 0.95
R7964:Tcaf2 UTSW 6 42,606,640 (GRCm39) missense probably benign
R8270:Tcaf2 UTSW 6 42,606,958 (GRCm39) missense probably benign 0.30
R8505:Tcaf2 UTSW 6 42,606,475 (GRCm39) missense probably benign 0.18
R8702:Tcaf2 UTSW 6 42,619,701 (GRCm39) missense probably benign 0.11
R8788:Tcaf2 UTSW 6 42,606,472 (GRCm39) missense probably damaging 1.00
R8979:Tcaf2 UTSW 6 42,601,404 (GRCm39) missense probably damaging 1.00
R9374:Tcaf2 UTSW 6 42,619,728 (GRCm39) missense probably benign 0.02
R9379:Tcaf2 UTSW 6 42,619,517 (GRCm39) missense probably benign 0.00
Y4339:Tcaf2 UTSW 6 42,606,406 (GRCm39) missense probably benign
Y4341:Tcaf2 UTSW 6 42,606,406 (GRCm39) missense probably benign
Z1177:Tcaf2 UTSW 6 42,606,550 (GRCm39) missense probably damaging 1.00
Posted On 2015-04-16